A. Bocoum

发表

An exploration of the genetics of the mutant Huntingtin (mHtt) gene in a cohort of patients with chorea from different tribes in 6 sub-Saharan African countries

H. Houlden, J. Hooker, N. Okubadejo, 2022, medRxiv.

A novel variant in the spatacsin gene causing SPG11 in a Malian family

K. Fischbeck, G. Landouré, O. Samassékou, 2020, Journal of the Neurological Sciences.

Hereditary spastic paraplegia type 35 in a family from Mali

K. Fischbeck, G. Landouré, O. Samassékou, 2019, American journal of medical genetics. Part A.

[Factors associated with mental disorders in the psychiatric department of the university hospital centre of Point G in Mali.]

G. Landouré, S. Coulibaly, A. Yalcouyé, 2021, Le Mali medical.

The State of Play of Parkinson's Disease in Africa: A Systematic Review and Point of View.

E. Hamid, O. Ojo, O. Okunoye, 2023, medRxiv.

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

Chelsea X Alvarado, D. Hernandez, M. Nalls, 2023, The Lancet Neurology.

The burden of headache and a health-care needs assessment in the adult population of Mali: a cross-sectional population-based study

G. Landouré, F. Konipo, H. Dolo, 2024, The journal of headache and pain.

The First Case of Huntington’s Disease like 2 in Mali, West Africa

G. Landouré, F. Essop, A. Krause, 2024, Tremor and other hyperkinetic movements.

Clinical and Genetic Aspects of Huntington's Disease in the Malian Population.

K. Fischbeck, G. Landouré, Y. Maiga, 2022, Journal of Huntington's disease.